Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,547 recalls have been distributed to West Virginia in the last 12 months.
Showing 3541–3560 of 27,884 recalls
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for...
The Issue: Devices were labeled with an expiration date of four years and ten days...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B-Intended to be used Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPince Ultra Full Core Biopsy Instrument: : 360-1080-01 Recalled by Argon...
The Issue: Holes have been identified in biopsy instrument packaging trays compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable 5 Lead Cable and Lead Wire System Recalled by Stryker...
The Issue: Disposable 5 lead cable and lead wire system package that should contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMINOS Lotus Max -Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max -Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max- Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multitom Rax -Intended to visualize anatomical structures by converting an...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis Recalled by...
The Issue: Affected product has an increased risk of postoperative perisprosthetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobra Recalled by Neurovision Medical Products Inc Due to Mislabeling
The Issue: mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.